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362 related items for PubMed ID: 18483067

  • 1. Mouse models of human KCNQ2 and KCNQ3 mutations for benign familial neonatal convulsions show seizures and neuronal plasticity without synaptic reorganization.
    Singh NA, Otto JF, Dahle EJ, Pappas C, Leslie JD, Vilaythong A, Noebels JL, White HS, Wilcox KS, Leppert MF.
    J Physiol; 2008 Jul 15; 586(14):3405-23. PubMed ID: 18483067
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  • 2. Electroconvulsive seizure thresholds and kindling acquisition rates are altered in mouse models of human KCNQ2 and KCNQ3 mutations for benign familial neonatal convulsions.
    Otto JF, Singh NA, Dahle EJ, Leppert MF, Pappas CM, Pruess TH, Wilcox KS, White HS.
    Epilepsia; 2009 Jul 15; 50(7):1752-9. PubMed ID: 19453707
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  • 3. Functional analysis of novel KCNQ2 mutations found in patients with Benign Familial Neonatal Convulsions.
    Volkers L, Rook MB, Das JH, Verbeek NE, Groenewegen WA, van Kempen MJ, Lindhout D, Koeleman BP.
    Neurosci Lett; 2009 Oct 02; 462(1):24-9. PubMed ID: 19559753
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  • 7. Genetic testing in benign familial epilepsies of the first year of life: clinical and diagnostic significance.
    Zara F, Specchio N, Striano P, Robbiano A, Gennaro E, Paravidino R, Vanni N, Beccaria F, Capovilla G, Bianchi A, Caffi L, Cardilli V, Darra F, Bernardina BD, Fusco L, Gaggero R, Giordano L, Guerrini R, Incorpora G, Mastrangelo M, Spaccini L, Laverda AM, Vecchi M, Vanadia F, Veggiotti P, Viri M, Occhi G, Budetta M, Taglialatela M, Coviello DA, Vigevano F, Minetti C.
    Epilepsia; 2013 Mar 02; 54(3):425-36. PubMed ID: 23360469
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  • 8. Conditional deletions of epilepsy-associated KCNQ2 and KCNQ3 channels from cerebral cortex cause differential effects on neuronal excitability.
    Soh H, Pant R, LoTurco JJ, Tzingounis AV.
    J Neurosci; 2014 Apr 09; 34(15):5311-21. PubMed ID: 24719109
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  • 9. Developmental changes in KCNQ2 and KCNQ3 expression in human brain: possible contribution to the age-dependent etiology of benign familial neonatal convulsions.
    Kanaumi T, Takashima S, Iwasaki H, Itoh M, Mitsudome A, Hirose S.
    Brain Dev; 2008 May 09; 30(5):362-9. PubMed ID: 18166285
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  • 12. KCNQ2 and KCNQ3 potassium channel genes in benign familial neonatal convulsions: expansion of the functional and mutation spectrum.
    Singh NA, Westenskow P, Charlier C, Pappas C, Leslie J, Dillon J, Anderson VE, Sanguinetti MC, Leppert MF, BFNC Physician Consortium.
    Brain; 2003 Dec 09; 126(Pt 12):2726-37. PubMed ID: 14534157
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  • 13. A spontaneous mutation involving Kcnq2 (Kv7.2) reduces M-current density and spike frequency adaptation in mouse CA1 neurons.
    Otto JF, Yang Y, Frankel WN, White HS, Wilcox KS.
    J Neurosci; 2006 Feb 15; 26(7):2053-9. PubMed ID: 16481438
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  • 15. Effects of KCNQ2 gene truncation on M-type Kv7 potassium currents.
    Robbins J, Passmore GM, Abogadie FC, Reilly JM, Brown DA.
    PLoS One; 2013 Feb 15; 8(8):e71809. PubMed ID: 23977150
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  • 16. Decreased subunit stability as a novel mechanism for potassium current impairment by a KCNQ2 C terminus mutation causing benign familial neonatal convulsions.
    Soldovieri MV, Castaldo P, Iodice L, Miceli F, Barrese V, Bellini G, Miraglia del Giudice E, Pascotto A, Bonatti S, Annunziato L, Taglialatela M.
    J Biol Chem; 2006 Jan 06; 281(1):418-28. PubMed ID: 16260777
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  • 17. Role of KCNQ2 and KCNQ3 genes in juvenile idiopathic epilepsy in Arabian foals.
    Lichter-Peled A, Polani S, Stanyon R, Rocchi M, Kahila Bar-Gal G.
    Vet J; 2013 Apr 06; 196(1):57-63. PubMed ID: 23182620
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  • 18. A novel mutation of KCNQ3 gene in a Chinese family with benign familial neonatal convulsions.
    Li H, Li N, Shen L, Jiang H, Yang Q, Song Y, Guo J, Xia K, Pan Q, Tang B.
    Epilepsy Res; 2008 Mar 06; 79(1):1-5. PubMed ID: 18249525
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  • 19. The first Korean case of KCNQ2 mutation in a family with benign familial neonatal convulsions.
    Yum MS, Ko TS, Yoo HW.
    J Korean Med Sci; 2010 Feb 06; 25(2):324-6. PubMed ID: 20119593
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  • 20. [A novel mutation in KCNQ2 gene causes benign familial infantile convulsions (BFIC) in a Chinese family].
    Zhou XH, Ma AQ, Liu XH, Huang C, Zhang YM, Shi RM.
    Zhonghua Er Ke Za Zhi; 2006 Jul 06; 44(7):487-91. PubMed ID: 17044971
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